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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1683986Erstellt: 26. Oktober 2026

Hydrochloric Acid → HCID 54300597, Verbindung

https://huagongshe.com/reaction/1683986

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktHydrochloric AcidHCID 313—
Edukt4-Bromobenzyl bromideHCID 68527—
Eduktmethyl 2-(5-methoxy-2-methyl-1H-indol-3-yl)acetateHCID 82067—
EduktPotassium bis(trimethylsilyl)amideHCID 3251421—
LösungsmittelTetrahydrofuranHCID 8028—
Lösungsmittel2(1H)-Pyrimidinone, tetrahydro-1,3-dimethyl-HCID 81646—
ProduktHCID 54300597HCID 5430059748%

Reaktionsbedingungen

Temperatur0 °C

Reaktionsschritte

To a solution of ester from Step 1 (13.8 g, 59 mmol) in THF (300 mL) and DMPU (40 mL) at -78° C. was added KHMDS solution (0.64M/toluene, 95 mL, 60 mmol). The reaction mixture was warmed to 0° C. and was then recooled to -78° C., at which point a solution of 4-bromobenzyl bromide (17.0 g, 68 mmol) in THF (80 mL) was added via double-tipped needle. The reaction was allowed to warm to r.t., and was then poured into 1M HCl (500 mL). The product was extracted with Et2O and the organic phase was washed with H2O and brine. After drying (MgSO4), filtration, and removal of solvent, the crude product was purified by flash chromatography (1:20 EtOAc/toluene). The resulting prodeuct was recrystallized from CH2Cl2 /hexane to give 11.4 g of the title compound.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05639780
Quelldatensatzuspto-grants-1997_06
ORD IDord-5d03c8c0fcdc4883b2d09df3cd31c2d3
Quellennotizuspto-grants-1997_06